Topological and energetic factors: what determines the structural details of the transition state ensemble and "en-route" intermediates for protein folding? An investigation for small globular proteins

J Mol Biol. 2000 May 19;298(5):937-53. doi: 10.1006/jmbi.2000.3693.

Abstract

Recent experimental results suggest that the native fold, or topology, plays a primary role in determining the structure of the transition state ensemble, at least for small, fast-folding proteins. To investigate the extent of the topological control of the folding process, we studied the folding of simplified models of five small globular proteins constructed using a Go-like potential to retain the information about the native structures but drastically reduce the energetic frustration and energetic heterogeneity among residue-residue native interactions. By comparing the structure of the transition state ensemble (experimentally determined by Phi-values) and of the intermediates with those obtained using our models, we show that these energetically unfrustrated models can reproduce the global experimentally known features of the transition state ensembles and "en-route" intermediates, at least for the analyzed proteins. This result clearly indicates that, as long as the protein sequence is sufficiently minimally frustrated, topology plays a central role in determining the folding mechanism.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Bacterial Proteins / chemistry
  • Bacterial Proteins / metabolism
  • Binding Sites
  • Computer Simulation*
  • Membrane Proteins / chemistry
  • Membrane Proteins / metabolism
  • Methyl-Accepting Chemotaxis Proteins
  • Molecular Weight
  • Peptides / chemistry
  • Peptides / metabolism
  • Plant Proteins
  • Protein Folding*
  • Protein Structure, Secondary
  • Proteins / chemistry*
  • Proteins / metabolism*
  • Ribonuclease H / chemistry
  • Ribonuclease H / metabolism
  • Ribonucleases / chemistry
  • Ribonucleases / metabolism
  • Temperature
  • Thermodynamics
  • src Homology Domains

Substances

  • Bacterial Proteins
  • Membrane Proteins
  • Methyl-Accepting Chemotaxis Proteins
  • Peptides
  • Plant Proteins
  • Proteins
  • chymotrypsin inhibitor 2
  • Ribonucleases
  • Ribonuclease H
  • Bacillus amyloliquefaciens ribonuclease